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FDA 510(k)

PRO-SHIATSU PORTABLE MASSAGER

K-Number: K940621 · 1994-06-22

Decision Date1994-06-22
Product CodeISA
Advisory CommitteePM
DecisionSubstantially Equivalent for Some Indications

Device Summary

PRO-SHIATSU PORTABLE MASSAGER is the device name listed in this FDA 510(k) record. The listed applicant is Westminster International Co., Inc.. It received FDA 510(k) clearance on 1994-06-22 under 510(k) number K940621. The device is classified under product code ISA. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent for Some Indications.

Frequently Asked Questions

What is the PRO-SHIATSU PORTABLE MASSAGER?

PRO-SHIATSU PORTABLE MASSAGER is a medical device that received FDA 510(k) clearance on 1994-06-22. The listed applicant is Westminster International Co., Inc.. The 510(k) number is K940621.

When did PRO-SHIATSU PORTABLE MASSAGER receive FDA 510(k) clearance?

PRO-SHIATSU PORTABLE MASSAGER received FDA 510(k) clearance on 1994-06-22, under 510(k) number K940621.

Who is the listed applicant for PRO-SHIATSU PORTABLE MASSAGER?

The FDA 510(k) record lists Westminster International Co., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PRO-SHIATSU PORTABLE MASSAGER?

The FDA product code for PRO-SHIATSU PORTABLE MASSAGER is ISA.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing Westminster International Co., Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Related Devices (Code: ISA)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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